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| 16.72, 17.02, 18.29, 22.43, 25.69, 30.24, 36.17, 36.77, 37.15, 41.36, 49.77, 52.04, 67.33, 75.81, 106.84, 120.5, 125.99, 126.14, 131.17, 135.43, 135.83, 137.71, 142.39, 148.6, 166.08, 167.42, 169.56 |
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1 . isoscalarafuran-A ÏàËÆ¶È:59.2% Chinese Journal of Natural Medicines 2003 1 137-141 Sesterterpenoids from Marine Sponges Hyrtios erectus QIU Yan; DENG Zhi-Wei; PEI Yue-Hu; FU Hong-Zheng; LIN Wen-Han Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . isoscalarafuran-A C27H40O4 ÏàËÆ¶È:59.2% Australian Journal of Chemistry 1993 46 1295-1299 Two New Scalarane Sesterterpenes: Isoscalarafuran-A and -B, Epimeric Alcohols From a Southern Australian Marine Sponge, Spongia hispida R Davis and RJ Capon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 11-epi-carnosiflogenin C C30H50O3 ÏàËÆ¶È:56.6% Chemical & Pharmaceutical Bulletin 1988 36 234-243 Glycosides from Chinese Medicinal Plant, Hemsleya panacis-scandens, and Structure-Taste Relationship of Cucurbitane Glycosides RYOJI KASAI,KAZUHIRO MATSUMOTO,RUI-LIN NIE,JUN ZHOU and OSAMU TANAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 8-epi-Ophiobolin J C25H36O4 ÏàËÆ¶È:55.5% Phytochemistry 2006 67 2281-2287 Ophiobolin E and 8-epi-ophiobolin J produced by Drechslera gigantea,a potential mycoherbicide of weedy grasses Antonio Evidente , Anna Andolfi, Alessio Cimmino, Maurizio Vurro, Mariano Fracchiolla, Raghavan Charudattan, Andrea Motta Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 7¦Á-acetyl-isopimara-8(14),15-dien-18-yl C26H38O6 ÏàËÆ¶È:55.5% Phytochemistry 1988 27 523-526 Terpenoids from Nepeta tuberosa subsp.reticulata (II) J.G. Urones,I. Sanchez Marcos,J. Ferna¡ändez Ferreras,P. Basabe Barcala Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Compound 7b ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry Letters 2000 10 1815-1818 A concise synthesis of photoactivatable 4-Aroyl-L-phenylalanines Enrico Morera, Giorgio Ortar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (2S,4aR,6aR,7R,9S,10aS,10bR)-methyl 9-acetoxy-2-(3-cyanobenzoyl)-6a,10b-dimethyl-4,10-dioxododecahydro-1H-benzo[f]isochromene-7-carboxylate C27H27NO8 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2012 20 3100-3110 Semisynthetic neoclerodanes as kappa opioid receptor probes Kimberly M. Lovell, Tamara Vasiljevik, Juan J. Araya, Anthony Lozama, Katherine M. Prevatt-Smith, Victor W. Day, Christina M. Dersch, Richard B. Rothman, Eduardo R. Butelman, Mary Jeanne Kreek, Thomas E. Prisinzano Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (2S,4aR,6aR,7R,9S,10aS,10bR)-methyl 9-acetoxy-6a,10bdimethyl-4,10-dioxo-2-(3-(tri-fluoromethoxy)benzoyl)dodecahydro-1H-benzo[f]isochromene-7-carboxylate C27H29F3O9 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2012 20 3100-3110 Semisynthetic neoclerodanes as kappa opioid receptor probes Kimberly M. Lovell, Tamara Vasiljevik, Juan J. Araya, Anthony Lozama, Katherine M. Prevatt-Smith, Victor W. Day, Christina M. Dersch, Richard B. Rothman, Eduardo R. Butelman, Mary Jeanne Kreek, Thomas E. Prisinzano Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 4-Acetoxydictyolactone C22H32O4 ÏàËÆ¶È:55.5% The Journal of Organic Chemistry 1988 53 5010-5013 Antitumor xenicane and norxenicane lactones from the brown alga Dictyota dichotoma Midori O. Ishitsuka, Takenori Kusumi, Hiroshi Kakisawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Ophiobolin J C25H38O4 ÏàËÆ¶È:55.5% The Journal of Organic Chemistry 1988 53 2170-2172 Some new phytotoxic ophiobolins produced by Drechslera oryzae Fumio Sugawara, Nobutaka Takahashi, Gary Strobel, Choong Hyo Yun, Gray George, Yali Fu, Jon Clardy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . (3aR,4aS,5aR,6aR)-octahydro-5a-methyl-3-methylidene-5-((3E)-3-{[(3-nitrobenzoyl)oxy]imino}-butyl)-2H-cyclopropa[f][1]benzofuran-2-one C22H24NNaO6 ÏàËÆ¶È:55.5% Chemistry & Biodiversity 2014 11 886-903 Semisynthesis and Antifungal Activity of Novel Oxime Ester Derivatives of Carabrone Modified at C(4) against Botrytis cinerea Delong Wang, Shuangxi Ren, Hao Wang, He Yan, Juntao Feng and Xing Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (3aR,4aS,5aR,6aR)-octahydro-5a-methyl-5-((3E)-3-{[(3-methylbenzoyl)oxy)imino}butyl)-3-methylidene-2H-cyclopropa[f][1]benzofuran-2-one C23H27NO4 ÏàËÆ¶È:55.5% Chemistry & Biodiversity 2014 11 886-903 Semisynthesis and Antifungal Activity of Novel Oxime Ester Derivatives of Carabrone Modified at C(4) against Botrytis cinerea Delong Wang, Shuangxi Ren, Hao Wang, He Yan, Juntao Feng and Xing Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (3aR,4aS,5aR,6aR)-octahydro-5a-methyl-3-methylidene-5-((3E)-3-{[(naphthalen-2-ylacetyl)oxy]imino}butyl)-2H-cyclopropa[f][1]benzofuran-2-one C27H29NO4 ÏàËÆ¶È:55.5% Chemistry & Biodiversity 2014 11 886-903 Semisynthesis and Antifungal Activity of Novel Oxime Ester Derivatives of Carabrone Modified at C(4) against Botrytis cinerea Delong Wang, Shuangxi Ren, Hao Wang, He Yan, Juntao Feng and Xing Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (3aR,4aS,5aR,6aR)-octahydro-5a-methyl-3-methylidene-5-[(3E)-3-({[(2E)-3-(4-nitrophenyl)prop-2-enoyl]oxy}imino)butyl]-2H-cyclopropa[f][1]benzofuran-2-one C24H26N2O6 ÏàËÆ¶È:55.5% Chemistry & Biodiversity 2014 11 886-903 Semisynthesis and Antifungal Activity of Novel Oxime Ester Derivatives of Carabrone Modified at C(4) against Botrytis cinerea Delong Wang, Shuangxi Ren, Hao Wang, He Yan, Juntao Feng and Xing Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 21-hydroxy-16-deacetyl-12-epi-scalarafuran acetate C27H40O4 ÏàËÆ¶È:55.5% Records of Natural Products 2014 4 417-421 Two New Scaralane-type Sesterterpenoids Isolated from the Marine Sponge Hyrtios erectus Lu Yin, Hui Li, Xiaoling Chen and Yan Qiu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (2S,4aR,6aR,7R,9S,10aS,10bR)-methyl 9-acetoxy-2-(benzothiophene-2-carbonyl)-6a,10b-dimethyl-4,10-dioxododecahydro-1H-benzo[f]isochromene-7-carboxylate C28H30O8S ÏàËÆ¶È:53.5% Bioorganic & Medicinal Chemistry 2012 20 3100-3110 Semisynthetic neoclerodanes as kappa opioid receptor probes Kimberly M. Lovell, Tamara Vasiljevik, Juan J. Araya, Anthony Lozama, Katherine M. Prevatt-Smith, Victor W. Day, Christina M. Dersch, Richard B. Rothman, Eduardo R. Butelman, Mary Jeanne Kreek, Thomas E. Prisinzano Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . (2S,4aR,6aR,7R,9S,10aS,10bR)-methyl 9-acetoxy-2-(benzothiophene-3-carbonyl)-6a,10b-dimethyl-4,10-dioxododecahydro-1H-benzo[f]isochromene-7-carboxylate C28H30O8S ÏàËÆ¶È:53.5% Bioorganic & Medicinal Chemistry 2012 20 3100-3110 Semisynthetic neoclerodanes as kappa opioid receptor probes Kimberly M. Lovell, Tamara Vasiljevik, Juan J. Araya, Anthony Lozama, Katherine M. Prevatt-Smith, Victor W. Day, Christina M. Dersch, Richard B. Rothman, Eduardo R. Butelman, Mary Jeanne Kreek, Thomas E. Prisinzano Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . (1S,3aS,41R,4a1S,5R,10aS,12aS)-1-(furan-3-yl)-3,8-bis(hydroxy-imino)-4a1,7,7,10a,12a-pentamethyl-1,3,3a,4a1,5,6,6a,7,8,10a,10b,11,12,12a-tetradecahydronaphtho[2,1-f]oxireno[2,3-d]isochromen-5-yl acetate C28H36N2O7 ÏàËÆ¶È:53.5% Journal of Medicinal Chemistry 2008 51 6495-6502 Gedunin, a Novel Hsp90 Inhibitor: Semisynthesis of Derivatives and Preliminary Structure−Activity Relationships Gary E. L. Brandt, Matthew D. Schmidt, Thomas E. Prisinzano and Brian S. J. Blagg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . scabronine H C27H36O5 ÏàËÆ¶È:51.8% Helvetica Chimica Acta 2004 Vol. 87 2877 Isolation and Characterization of New Bitter Diterpenoids from the Basidiomycete Sarcodon scabrosus Bing-Ji Ma, Hua-Jie Zhu, and Ji-Kai Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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